Canonical Allele Identifier: CA2716180119
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs2116850434

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150861362_150861363insAA , CM000669.2:g.150861362_150861363insAA GRCh38
NC_000007.13:g.150558450_150558451insAA , CM000669.1:g.150558450_150558451insAA GRCh37
NC_000007.12:g.150189383_150189384insAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.*153_*154insAA MANE Select ENSP00000354193.4:n.*153_*154insAA
ENST00000360937.8:c.*153_*154insAA ENSP00000354193.4:n.*153_*154insAA
ENST00000467291.5:c.*153_*154insAA ENSP00000418328.1:n.*153_*154insAA
ENST00000493429.5:c.*153_*154insAA ENSP00000418614.1:n.*153_*154insAA
XR_928169.1:n.295+15647_295+15648insTT
XR_928170.1:n.425+7254_425+7255insTT
XR_928171.1:n.297+15647_297+15648insTT
XR_928169.2:n.301+15647_301+15648insTT
XR_928171.2:n.301+15647_301+15648insTT
NM_001091.4:c.*153_*154insAA MANE Select NP_001082.2:n.*153_*154insAA
NM_001272072.2:c.*153_*154insAA NP_001259001.1:n.*153_*154insAA